Gene entry
HSPB1
heat shock protein family B (small) member 1
- Chromosome
- 7
- Cytoband
- 7q11.23
- Variants (rsID)
- 4
HSPB1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7q11.23). Its official name is “heat shock protein family B (small) member 1”. The reference table lists 4 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs199602956Benignsingle nucleotide variantNeuronopathy, distal hereditary motor, type 2B|Charcot-Marie-Tooth disease axonal type 2F|Charcot-Marie-Tooth disease
- rs201769668Benignsingle nucleotide variantNeuronopathy, distal hereditary motor, type 2B|Charcot-Marie-Tooth disease axonal type 2F
- rs367662394Conflicting interpretationssingle nucleotide variantCharcot-Marie-Tooth disease axonal type 2F|Charcot-Marie-Tooth disease
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.